Informacija apie narį
Pr José-Alain Sahel
Prancūzija
Komanda
Pr Isabelle Audo
Prancūzija
Dr Christina Zeitz
Prancūzija
Dr Catherine Vignal-Clermont
Prancūzija
HCP centras
kontaktas
RÉFÉRET National Hospital of Ophthalmology of Quinze-Vingts, Paris, France
Klinikiniai tyrimai
A Post-Authorization, Multicenter, Multinational, Longitudinal,Observational Safety Registry Study for Patients Treated with Voretigene Neparvovec.
A Study to Determine the Long Term Safety, Tolerability and Biological Activity of SAR422459 in Patients With Stargardt’s Macular Degeneration.
An Open-Label Study to Determine the Long Term Safety, Tolerability and Biological Activity of UshStat® in Patients With Usher Syndrome Type 1B.
Argus® II Retinal Prosthesis System: Post-Market Study
Argus® II Retinal Stimulation System Feasibility Protocol.
Autosomal Dominant Retinitis Pigmentosa: Prevalence of Known Genes Identification of New Loci/Genes.
Clinical and Genetic Examination of Usher Syndrome Patients’ Cohort in Europe.
Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy.
Leber Hereditary Optic Neuropathy (LHON) Historical Case Record Survey.
Phase I/IIa Study of SAR422459 in Patients With Stargardt’s Macular Degeneration.
Prospective Natural History Study of Retinitis Pigmentosa (PHENOROD2)
Study of UshStat in Patients With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B.
Prospective study of visual function in USHER syndrome induced by MYO7A mutation and retinotosis pigmentosa.
Mokslinės publikacijos
Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F‐mediated inherited retinal disorders
Išsamus tyrimas, taikant tiesioginį Sangerio genus koduojančių regionų seką, egzomo ir genomo seką, taikomą didelei grupei...
Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years
Kiekybiniai SP rodikliai žymiai sumažėjo per 2 metus su USH2A susijusioje tinklainėje...
Shedding light on myopia by studying complete congenital stationary night blindness
Rezultatai yra pagrindas farmakologinės trumparegystės vystymuisi...